Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Operations GmbH@Evonik Rexim SAS
01 1Hyundai Pharmaceutical Co., Ltd.
01 1Lisinopril dihydrate
01 1Germany
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registrant Name : Hyundai Pharmaceutical Co., Ltd.
Registration Date : 2021-05-14
Registration Number : 20210514-209-J-989
Manufacturer Name : Evonik Operations GmbH@Evoni...
Manufacturer Address : Rodenbacher Chaussee 4 63457 Hanau Germany@33 rue de Verdun 80400 Ham, FRANCE
A ZESTRIL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZESTRIL, including repackagers and relabelers. The FDA regulates ZESTRIL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZESTRIL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of ZESTRIL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ZESTRIL supplier is an individual or a company that provides ZESTRIL active pharmaceutical ingredient (API) or ZESTRIL finished formulations upon request. The ZESTRIL suppliers may include ZESTRIL API manufacturers, exporters, distributors and traders.
click here to find a list of ZESTRIL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a ZESTRIL Drug Master File in Korea (ZESTRIL KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of ZESTRIL. The MFDS reviews the ZESTRIL KDMF as part of the drug registration process and uses the information provided in the ZESTRIL KDMF to evaluate the safety and efficacy of the drug.
After submitting a ZESTRIL KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their ZESTRIL API can apply through the Korea Drug Master File (KDMF).
click here to find a list of ZESTRIL suppliers with KDMF on PharmaCompass.
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